• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伏隔核中胆囊收缩素拮抗剂对黑暗诱导的活动亢进的抑制作用。

Attenuation of dark-induced hyperlocomotion by a cholecystokinin antagonist in the nucleus accumbens.

作者信息

Crawley J N

机构信息

Clinical Neuroscience Branch, National Institute of Mental Health, Bethesda, MD 20892.

出版信息

Brain Res. 1988 Nov 15;473(2):398-400. doi: 10.1016/0006-8993(88)90874-8.

DOI:10.1016/0006-8993(88)90874-8
PMID:3233498
Abstract

A dark-induced hyperlocomotion paradigm was developed to investigate the role of endogenous cholecystokinin in mediating exploratory locomotor activity in the mesolimbic pathway, where cholecystokinin coexists with dopamine. Microinjection of the cholecystokinin receptor antagonist, proglumide, 10-20 micrograms, into the medial posterior nucleus accumbens, significantly inhibited dark-induced hyperlocomotion, while having no effect on locomotion in the light. These data suggest that endogenous cholecystokinin contributes to behaviorally relevant functions of the activated mesolimbic pathway.

摘要

为了研究内源性胆囊收缩素在介导中脑边缘通路探索性运动活动中的作用,开发了一种黑暗诱导的运动亢进范式,在该通路中胆囊收缩素与多巴胺共存。向伏隔核内侧后核微量注射10 - 20微克胆囊收缩素受体拮抗剂丙谷胺,可显著抑制黑暗诱导的运动亢进,而对光照下的运动没有影响。这些数据表明内源性胆囊收缩素有助于激活的中脑边缘通路的行为相关功能。

相似文献

1
Attenuation of dark-induced hyperlocomotion by a cholecystokinin antagonist in the nucleus accumbens.伏隔核中胆囊收缩素拮抗剂对黑暗诱导的活动亢进的抑制作用。
Brain Res. 1988 Nov 15;473(2):398-400. doi: 10.1016/0006-8993(88)90874-8.
2
Subtype-selective cholecystokinin receptor antagonists block cholecystokinin modulation of dopamine-mediated behaviors in the rat mesolimbic pathway.亚型选择性胆囊收缩素受体拮抗剂可阻断胆囊收缩素对大鼠中脑边缘通路中多巴胺介导行为的调节作用。
J Neurosci. 1992 Sep;12(9):3380-91. doi: 10.1523/JNEUROSCI.12-09-03380.1992.
3
Antagonism of cholecystokinin function in the rostral and caudal nucleus accumbens: differential effects on brain stimulation reward.
Neurosci Lett. 1989 Feb 13;97(1-2):151-6. doi: 10.1016/0304-3940(89)90155-9.
4
Cholecystokinin antagonist lorglumide reverses chronic haloperidol-induced effects on dopamine neurons.
Brain Res. 1988 Nov 8;473(1):165-8. doi: 10.1016/0006-8993(88)90330-7.
5
Antagonists of central and peripheral behavioral actions of cholecystokinin octapeptide.胆囊收缩素八肽中枢和外周行为作用的拮抗剂。
J Pharmacol Exp Ther. 1986 Feb;236(2):320-30.
6
Behavioral evidence for cholecystokinin modulation of dopamine in the mesolimbic pathway.胆囊收缩素对中脑边缘通路多巴胺调节作用的行为学证据。
Prog Clin Biol Res. 1985;192:131-8.
7
Nucleus accumbens cholecystokinin (CCK) can either attenuate or potentiate amphetamine-induced locomotor activity: evidence for rostral-caudal differences in accumbens CCK function.伏隔核胆囊收缩素(CCK)可减弱或增强苯丙胺诱导的运动活性:伏隔核CCK功能存在头端-尾端差异的证据。
Behav Neurosci. 1989 Aug;103(4):831-6.
8
Antagonism by haloperidol of the suppression of exploratory locomotor activity induced by the local application of (-)3-(3-hydroxyphenyl)-N-n-propylpiperidine into the nucleus accumbens of the rat.
Experientia. 1984 Aug 15;40(8):858-9. doi: 10.1007/BF01951994.
9
Topographical analysis of nucleus accumbens sites at which cholecystokinin potentiates dopamine-induced hyperlocomotion in the rat.
Brain Res. 1985 Jun 3;335(2):337-41. doi: 10.1016/0006-8993(85)90489-5.
10
Low doses of accumbens dopamine modulate amygdala suppression of spontaneous exploratory activity in rats.低剂量伏隔核多巴胺调节大鼠杏仁核对自发探索活动的抑制作用。
Brain Res. 1989 Jan 16;477(1-2):202-10. doi: 10.1016/0006-8993(89)91408-x.

引用本文的文献

1
The use of sudden darkness in mice: a behavioural and pharmacological approach.在小鼠中使用突然变暗:一种行为学和药理学方法。
Psychopharmacology (Berl). 2005 Jun;179(4):846-53. doi: 10.1007/s00213-004-2107-0. Epub 2004 Dec 24.